Clinical Study of Aspirin and Zileuton on Biomarkers of Tobacco-Related Carcinogenesis in Current Smokers
Author
Garland, L.L.Guillen-Rodriguez, J.
Hsu, C.-H.
Davis, L.E.
Szabo, E.
Husted, C.R.
Liu, H.
Leclerc, A.
Alekseyev, Y.O.
Liu, G.
Bauman, J.E.
Spira, A.E.
Beane, J.
Wojtowicz, M.
Chow, H.-H.S.
Affiliation
Department of Medicine, University of ArizonaUniversity of Arizona Cancer Center, University of Arizona
College of Pharmacy, University of Arizona
Issue Date
2022
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MDPICitation
Garland, L. L., Guillen-Rodriguez, J., Hsu, C.-H., Davis, L. E., Szabo, E., Husted, C. R., Liu, H., Leclerc, A., Alekseyev, Y. O., Liu, G., Bauman, J. E., Spira, A. E., Beane, J., Wojtowicz, M., & Chow, H.-H. S. (2022). Clinical Study of Aspirin and Zileuton on Biomarkers of Tobacco-Related Carcinogenesis in Current Smokers. Cancers, 14(12).Journal
CancersRights
Copyright © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
The chemopreventive effect of aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) on lung cancer risk is supported by epidemiologic and preclinical studies. Zileuton, a 5-lipoxygenase inhibitor, has additive activity with NSAIDs against tobacco carcinogenesis in preclinical models. We hypothesized that cyclooxygenase plus 5-lipoxygenase inhibition would be more effective than a placebo in modulating the nasal epithelium gene signatures of tobacco exposure and lung cancer. We conducted a randomized, double-blinded study of low-dose aspirin plus zileuton vs. double placebo in current smokers to compare the modulating effects on nasal gene expression and arachidonic acid metabolism. In total, 63 participants took aspirin 81 mg daily plus zileuton (Zyflo CR) 600 mg BID or the placebo for 12 weeks. Nasal brushes from the baseline, end-of-intervention, and one-week post intervention were profiled via microarray. Aspirin plus zilueton had minimal effects on the modulation of the nasal or bronchial gene expression signatures of smoking, lung cancer, and COPD but favorably modulated a bronchial gene expression signature of squamous dysplasia. Aspirin plus zileuton suppressed urinary leukotriene but not prostaglandin E2, suggesting shunting through the cyclooxygenase pathway when combined with 5-lipoxygenase inhibition. Continued investigation of leukotriene inhibitors is needed to confirm these findings, understand the long-term effects on the airway epithelium, and identify the safest, optimally dosed agents. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.Note
Open access journalISSN
2072-6694Version
Final published versionae974a485f413a2113503eed53cd6c53
10.3390/cancers14122893
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Except where otherwise noted, this item's license is described as Copyright © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).